4.5 Article

Polymeric Nanoparticles for Increased Oral Bioavailability and Rapid Absorption Using Celecoxib as a Model of a Low-Solubility, High-Permeability Drug

Related references

Note: Only part of the references are listed.
Article Chemistry, Medicinal

The Developability Classification System: Application of Biopharmaceutics Concepts to Formulation Development

James M. Butler et al.

JOURNAL OF PHARMACEUTICAL SCIENCES (2010)

Article Pharmacology & Pharmacy

Advantages of celecoxib nanosuspension formulation and transformation into tablets

Andrej Dolenc et al.

INTERNATIONAL JOURNAL OF PHARMACEUTICS (2009)

Article Pharmacology & Pharmacy

A Model-Based Methodology for Spray-Drying Process Development

Dan E. Dobry et al.

JOURNAL OF PHARMACEUTICAL INNOVATION (2009)

Article Pharmacology & Pharmacy

Enhancing intestinal drug solubilisation using lipid-based delivery systems

Christopher J. H. Porter et al.

ADVANCED DRUG DELIVERY REVIEWS (2008)

Article Pharmacology & Pharmacy

High bioavailability from nebulized itraconazole nanoparticle dispersions with biocompatible stabilizers

Wei Yang et al.

INTERNATIONAL JOURNAL OF PHARMACEUTICS (2008)

Review Pharmacology & Pharmacy

Top-down production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products

Bernard Van Eerdenbrugh et al.

INTERNATIONAL JOURNAL OF PHARMACEUTICS (2008)

Article Medicine, Research & Experimental

Hydroxypropyl Methylcellulose Acetate Succinate-Based Spray-Dried Dispersions: An Overview

Dwayne T. Friesen et al.

MOLECULAR PHARMACEUTICS (2008)

Review Chemistry, Multidisciplinary

Pharmaceutical particle engineering via spray drying

Reinhard Vehring

PHARMACEUTICAL RESEARCH (2008)

Review Pharmacology & Pharmacy

Oral lipid-based formulations

David J. Hauss

ADVANCED DRUG DELIVERY REVIEWS (2007)

Review Pharmacology & Pharmacy

Freeze-drying of nanoparticles: Formulation, process and storage considerations

Wassim Abdelwahed et al.

ADVANCED DRUG DELIVERY REVIEWS (2006)

Review Medicine, Research & Experimental

Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs

RN Gursoy et al.

BIOMEDICINE & PHARMACOTHERAPY (2004)

Article Pharmacology & Pharmacy

Characterization of solid-state forms of celecoxib

G Chawla et al.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2003)

Review Pharmacology & Pharmacy

Amorphous pharmaceutical solids: preparation, characterization and stabilization

L Yu

ADVANCED DRUG DELIVERY REVIEWS (2001)

Article Pharmacology & Pharmacy

Drug-like properties and the causes of poor solubility and poor permeability

CA Lipinski

JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS (2000)

Review Pharmacology & Pharmacy

Improving drug solubility for oral delivery using solid dispersions

C Leuner et al.

EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2000)

Article Chemistry, Multidisciplinary

What is the true solubility advantage for amorphous pharmaceuticals?

BC Hancock et al.

PHARMACEUTICAL RESEARCH (2000)